
Immunity, Journal Year: 2018, Volume and Issue: 48(1), P. 19 - 33
Published: Jan. 1, 2018
Language: Английский
Immunity, Journal Year: 2018, Volume and Issue: 48(1), P. 19 - 33
Published: Jan. 1, 2018
Language: Английский
Cell, Journal Year: 2016, Volume and Issue: 165(6), P. 1332 - 1345
Published: June 1, 2016
Language: Английский
Citations
4996Cell, Journal Year: 2017, Volume and Issue: 169(3), P. 381 - 405
Published: April 1, 2017
Language: Английский
Citations
3027Cell, Journal Year: 2012, Volume and Issue: 149(1), P. 22 - 35
Published: March 1, 2012
Language: Английский
Citations
2933Nature reviews. Immunology, Journal Year: 2016, Volume and Issue: 16(9), P. 553 - 565
Published: July 11, 2016
Language: Английский
Citations
2469Immunity, Journal Year: 2011, Volume and Issue: 35(6), P. 871 - 882
Published: Dec. 1, 2011
Language: Английский
Citations
1892Immunity, Journal Year: 2013, Volume and Issue: 38(4), P. 633 - 643
Published: April 1, 2013
Language: Английский
Citations
1415Cell, Journal Year: 2011, Volume and Issue: 146(5), P. 772 - 784
Published: Aug. 27, 2011
Language: Английский
Citations
1414Science, Journal Year: 2013, Volume and Issue: 342(6155)
Published: Oct. 10, 2013
Lymphocytes face major metabolic challenges upon activation. They must meet the bioenergetic and biosynthetic demands of increased cell proliferation also adapt to changing environmental conditions, in which nutrients oxygen may be limiting. An emerging theme immunology is that reprogramming lymphocyte activation are intricately linked. However, why T cells adopt specific programs impact these have on function and, ultimately, immunological outcome remain unclear. Research tumor metabolism has provided valuable insight into pathways important for influence metabolites themselves signal transduction epigenetic programming. In this Review, we highlight concepts regarding proliferating discuss their potential fate function.
Language: Английский
Citations
1219Annual Review of Immunology, Journal Year: 2013, Volume and Issue: 31(1), P. 259 - 283
Published: Jan. 9, 2013
T cell activation leads to dramatic shifts in metabolism protect against pathogens and orchestrate the action of other immune cells. Quiescent cells require predominantly ATP-generating processes, whereas proliferating effector high metabolic flux through growth-promoting pathways. Further, functionally distinct subsets energetic biosynthetic pathways support their specific functional needs. Pathways that control function are intimately linked, changes at both system levels have been shown enhance or suppress functions. As a result these findings, is now appreciated as key regulator specification fate. This review discusses role cellular development, activation, differentiation, highlight clinical relevance opportunities for therapeutic interventions may be used disrupt pathogenesis.
Language: Английский
Citations
1141Nature, Journal Year: 2013, Volume and Issue: 493(7432), P. 346 - 355
Published: Jan. 15, 2013
Language: Английский
Citations
1056